Canonical Allele Identifier: CA1801418146
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89943276C= , CM000670.2:g.89943276C= GRCh38
NC_000008.10:g.90955504C= , CM000670.1:g.90955504C= GRCh37
NC_000008.9:g.91024680C= NCBI36
NG_008860.1:g.46396G= , LRG_158:g.46396G=

Transcript Alleles

HGVS Amino-acid Change
NM_002485.5:c.2161G= MANE Select NP_002476.2:p.Glu721=
ENST00000265433.8:c.2161G= MANE Select ENSP00000265433.4:p.Glu721=
NM_001024688.2:c.1915G= NP_001019859.1:p.Glu639=
NM_001024688.3:c.1915G= NP_001019859.1:p.Glu639=
NM_002485.4:c.2161G= , LRG_158t1:c.2161G= NP_002476.2:p.Glu721=
ENST00000265433.7:c.2161G= ENSP00000265433.3:p.Glu721=
ENST00000396252.6:c.*2034G= ENSP00000379551.2:n.*2034G=
ENST00000409330.5:c.1915G= ENSP00000386924.1:p.Glu639=
ENST00000494804.2:n.3463G=
ENST00000517337.2:c.1915G= ENSP00000429971.2:p.Glu639=
ENST00000523444.2:c.1915G= ENSP00000428252.2:p.Glu639=
ENST00000613033.1:c.271G= ENSP00000484487.1:p.Glu91=
ENST00000697292.1:c.2161G= ENSP00000513229.1:p.Glu721=
ENST00000697293.1:c.2161G= ENSP00000513230.1:p.Glu721=
ENST00000697294.1:c.*1772G= ENSP00000513231.1:n.*1772G=
ENST00000697295.1:c.*1470G= ENSP00000513232.1:n.*1470G=
ENST00000697296.1:c.*1829G= ENSP00000513233.1:n.*1829G=
ENST00000697297.1:n.3946G=
ENST00000697298.1:c.1915G= ENSP00000513234.1:p.Glu639=
ENST00000697299.1:c.1915G= ENSP00000513235.1:p.Glu639=
ENST00000697300.1:c.*1765G= ENSP00000513236.1:n.*1765G=
ENST00000697301.1:c.*1682G= ENSP00000513237.1:n.*1682G=
ENST00000697302.1:c.*1682G= ENSP00000513238.1:n.*1682G=
ENST00000697303.1:c.*1765G= ENSP00000513239.1:n.*1765G=
ENST00000697304.1:c.1849G= ENSP00000513240.1:p.Glu617=
ENST00000697305.1:n.2428G=
ENST00000697306.1:c.*2712G= ENSP00000513241.1:n.*2712G=
ENST00000697307.1:c.1936G= ENSP00000513242.1:p.Glu646=
ENST00000697308.1:c.2092G= ENSP00000513243.1:p.Glu698=
ENST00000697309.1:c.2161G= ENSP00000513244.1:p.Glu721=
ENST00000697310.1:c.2161G= ENSP00000513245.1:p.Glu721=
ENST00000697311.1:c.2161G= ENSP00000513246.1:p.Glu721=
ENST00000697312.1:c.*1559G= ENSP00000513247.1:n.*1559G=
ENST00000697313.1:n.2688-7664G=
ENST00000697314.1:n.3637-7664G=
ENST00000697315.1:c.2161G= ENSP00000513248.1:p.Glu721=
ENST00000697316.1:n.2282G=
XM_011517044.1:c.2137G= XP_011515346.1:p.Glu713=
XM_011517045.1:c.1915G= XP_011515347.1:p.Glu639=
XM_017013460.1:c.1282G= XP_016868949.1:p.Glu428=
XM_017013462.2:c.1282G= XP_016868951.1:p.Glu428=
XM_024447163.1:c.1915G= XP_024302931.1:p.Glu639=
XM_024447164.1:c.1915G= XP_024302932.1:p.Glu639=
XM_024447165.1:c.1282G= XP_024302933.1:p.Glu428=